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Showing results (31-40 of 38) with videos related to

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Pediatric Pulmonology|November 9, 2004
Trampoline use as physiotherapy for cystic fibrosis patientsA Barak, I D Wexler, O Efrati, et al.
Pediatrics|April 3, 1998
A missense cystic fibrosis transmembrane conductance regulator mutation with variable phenotypeE Kerem, M Nissim-Rafinia, Z Argaman, et al.
International Journal of Clinical & Laboratory Research|January 8, 1999
Serum lipase levels pre and post Lundh meal: evaluation of exocrine pancreatic status in cystic fibrosisA Augarten, D Katznelson, L Dubenbaum, et al.
Pediatric Pulmonology|October 3, 2000
Serum lipase levels as a diagnostic marker in cystic fibrosis patients with normal or borderline sweat testsA Augarten, H Shmilovich, R Doolman, et al.
Pediatric Transplantation|September 19, 2001
Prediction of mortality and timing of referral for lung transplantation in cystic fibrosis patientsA Augarten, H Akons, M Aviram, et al.
The European Respiratory Journal|August 9, 2001
Nasal potential difference measurements in patients with atypical cystic fibrosisM Wilschanski, H Famini, N Strauss-Liviatan, et al.
Clinical and Experimental Medicine|November 5, 2003
Serum CA 19-9 levels as a diagnostic marker in cystic fibrosis patients with borderline sweat testsA Augarten, H Berman, M Aviram, et al.
American Journal of Respiratory and Critical Care Medicine|June 1, 1997
A cystic fibrosis transmembrane conductance regulator splice variant with partial penetrance associated with variable cystic fibrosis presentationsE Kerem, N Rave-Harel, A Augarten, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Pediatric Pulmonology|November 9, 2004
Trampoline use as physiotherapy for cystic fibrosis patientsA Barak, I D Wexler, O Efrati, et al.
Pediatrics|April 3, 1998
A missense cystic fibrosis transmembrane conductance regulator mutation with variable phenotypeE Kerem, M Nissim-Rafinia, Z Argaman, et al.
International Journal of Clinical & Laboratory Research|January 8, 1999
Serum lipase levels pre and post Lundh meal: evaluation of exocrine pancreatic status in cystic fibrosisA Augarten, D Katznelson, L Dubenbaum, et al.
Pediatric Pulmonology|October 3, 2000
Serum lipase levels as a diagnostic marker in cystic fibrosis patients with normal or borderline sweat testsA Augarten, H Shmilovich, R Doolman, et al.
Pediatric Transplantation|September 19, 2001
Prediction of mortality and timing of referral for lung transplantation in cystic fibrosis patientsA Augarten, H Akons, M Aviram, et al.
The European Respiratory Journal|August 9, 2001
Nasal potential difference measurements in patients with atypical cystic fibrosisM Wilschanski, H Famini, N Strauss-Liviatan, et al.
Clinical and Experimental Medicine|November 5, 2003
Serum CA 19-9 levels as a diagnostic marker in cystic fibrosis patients with borderline sweat testsA Augarten, H Berman, M Aviram, et al.
American Journal of Respiratory and Critical Care Medicine|June 1, 1997
A cystic fibrosis transmembrane conductance regulator splice variant with partial penetrance associated with variable cystic fibrosis presentationsE Kerem, N Rave-Harel, A Augarten, et al.
Pageof 4